| Literature DB >> 29141479 |
Liang Hong1, Chuan-Li Zhou2, Feng-Ping Chen1, Dan Han1, Chun-Yuan Wang1, Jia-Xin Li1, Zhe Chi1, Chen-Guang Liu1.
Abstract
In this research, firstly astaxanthin (ASX)-loaded nanoemulsions (NEs) were produced using a convenient low-energy emulsion phase inversion method. The optimised ASX-NEs were prepared in the presence of Cremophor® EL and Labrafil® M 1944 CS, with a surfactant-to-oil ratio of 4:6. The ASX-NE droplets were spherical with a mean droplet diameter below 100 nm and a small negative surface charge. The system was stable without alteration of mean droplet diameter for three months. Then, the ASX-NE was functionalised with carboxymethyl chitosan (CMCS) through direct CMCS (0.02%) incorporation during the preparation process. The ASX chemical stability and skin permeability increased in the following order: ASX solution control < ASX-NE < CMCS-ASX-NE. Cell viability assays on L929 cells revealed low cytotoxicity of blank NE, ASX-NE and CMCS-ASX-NE in the range from 5 to 500 μg mL-1. In conclusion, the CMCS-ASX-NE might be a promising delivery vehicle in dermal and transdermal products.Entities:
Keywords: Transdermal; astaxanthin; carboxymethyl chitosan; low-energy; nanoemulsion; stability
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Year: 2017 PMID: 29141479 DOI: 10.1080/02652048.2017.1373154
Source DB: PubMed Journal: J Microencapsul ISSN: 0265-2048 Impact factor: 3.142